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Reagent Production Analyst

Company: Cepheid
Location: Sunnyvale
Posted on: November 22, 2021

Job Description:

Mid level position responsible for supporting the Bulk Buffer, Reagents and Bead production laboratories by following good documentation practices (cGDP) and relevant standard operating procedures (SOPs). Complete assigned tasks and ensure all activities are compliant with the company's quality, safety and departmental policies and standards. Apply analytical skills or scientific methods or operational processes to perform activities with a moderate degree of supervision.
Work safely with hazardous chemicals and follow all safety policies fostering a safe work environment
Immediately report all safety concerns including injuries and safety suggestions
Recognizes and solves typical problems that can occur in own work area without supervisory approval; evaluates and selects solutions from established operating procedures and/or scientific methods
Responsible for: liquid bead formulation, bulk buffer formulation, bead dropping using a beadulator, loading and unloading beads from the lyophilizer, sieving of beads, aliquoting and labeling of dyes and grease
Performs pH, Moisture, Conductivity and Density testing
Perform accurate real time documentation to ensure right first time (RFT) operations
Perform verification and review of peer activities
Train others on lab responsibilities
Monitor equipment and inform leads or management of any issues
Maintain laboratory housekeeping including reagent and equipment inventory levels
Recognize issues and defects and complete necessary documentation and escalate accordingly
Recommend and implement improvement ideas in the lab that will positively affect production efficiency, Quality and Safety
Assist other department in qualification of new methods and instruments
Trouble shoot equipment and assay failures
Suggest and assist in SOP revisions
Complete all assigned and required training satisfactorily and on time
Education and Experience:
High School degree (or equivalent experience) with 2-4 years of related work experience OR
AA or Technical Trade Degree with 1-2 years of work experience
Knowledge and skills:
Must be able to follow cGMP and cGLPs, FDA and ISO standards
Must be able to follow direction, able to understand SOPs and demonstrate understanding through speech and/or written form
Proficiency in computer systems such as Word, Excel, SAP and e-mail
Has good understanding of how the team integrates with others
Applies experience and skills to complete assigned work within area of expertise
Physical requirements/abilities:
Must be able to lift 25 Lb Must be able to stand for several hours. Work may involve repetitive arm/wrist motions
Ability to transport heavy materials up to 400 Lb with the appropriate machine or equipment assist
Ability to work in a controlled environment
Bachelor's Degree in Life Sciences
Experience working in a GMP/ISO manufacturing environment
Experience using analytical scales, Pipettes and working with hazardous chemicals
Flexibility with the work schedule including modified shift times, overtime and weekends

When you join us, you'll also be joining Danaher's global organization, where 69,000 people wake up every day determined to help our customers win. As an associate, you'll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful Danaher Business System tools and the stability of a tested organization.

Danaher Corporation and all Danaher Companies require all US and Puerto Rico employees to be vaccinated against COVID-19 as a condition of employment, subject to reasonable accommodation as required by law.

Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. - Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

The EEO posters are available here .

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at to request accommodation.

If you've ever wondered what's within you, there's no better time to find out.

Keywords: Cepheid, Sunnyvale , Reagent Production Analyst, Professions , Sunnyvale, California

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